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Not yet recruiting Phase 2 Interventional

A Clinical Study of Ixazomib to Reactivate HIV and Reduce HIV Reservoir Size

ClinicalTrials.gov ID: NCT07881809

Public ClinicalTrials.gov record NCT07881809. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 1:39 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Double-Blinded, Randomized, Placebo-Controlled Trial of Ixazomib to Reactivate HIV and Reduce HIV Reservoir Size

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study tests whether a medicine called ixazomib is safe for people living with HIV, and whether it can wake up HIV that is hiding in the body so the immune system and treatment can reach it. HIV can stay hidden inside cells even when antiretroviral therapy (ART) keeps the virus under control. These hidden cells are called the HIV reservoir, and they are the reason HIV is not cured by ART alone. Laboratory research suggests ixazomib may reactivate hidden HIV and also help kill the cells that carry it. Ixazomib is already approved to treat a cancer called multiple myeloma and has been given to a smaller group of people with HIV in an earlier study. About 45 adults with HIV that is well controlled on ART will take part. Participants are assigned by chance to take either ixazomib or a placebo - a capsule with no active medicine - one capsule by mouth once a week for a total of 25 doses. Two out of every three participants receive ixazomib and one out of three receives placebo. Neither participants nor the study staff know which one a participant is taking. Everyone continues their own HIV treatment throughout the study. Participation lasts about 7 months: 24 weeks of weekly capsules and 4 more weeks of follow-up after the last dose. Participants come to the clinic for about 14 visits, and take their capsule 24 to 36 hours before each visit so blood samples can show the effect of the dose. The main purposes of the study are to evaluate whether ixazomib is safe and tolerable, and to measure whether it increases the very small amounts of HIV in the blood compared with placebo. The study also measures the size of the HIV reservoir and how the immune system responds.

Study identification

NCT ID
NCT07881809
Recruitment status
Not yet recruiting
Study type
Interventional
Phase
Phase 2
Enrollment
45 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 23, 2026 (Estimated)
Primary completion
Oct 8, 2027 (Estimated)
Completion
Nov 5, 2027 (Estimated)
Last update posted
Oct 19, 2026

2026 – 2027

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
Alabama CRS (Site #31788) Birmingham Alabama 35222 —
University of California, Los Angeles CARE Center CRS (Site #601) Los Angeles California 90035 —
UCSD Antiviral Research Center CRS (Site #701) San Diego California 92103 —
University of California, San Francisco HIV/AIDS CRS (Site #801) San Francisco California 94110 —
University of Colorado Hospital CRS (Site #6101) Aurora Colorado 80045 —
Whitman-Walker Institute, Inc. CRS (Site #31791) Washington D.C. District of Columbia 20009 —
The Ponce de Leon Center CRS (Site #5802) Atlanta Georgia 30308-2012 —
Northwestern University CRS (Site #2701) Chicago Illinois 60611 —
Massachusetts General Hospital CRS (MGH CRS) (Site #101) Boston Massachusetts 02114 —
Columbia Physicians & Surgeons (P&S) CRS (Site #30329) New York New York 10032 —
University of Rochester Adult HIV Therapeutic Strategies Network CRS (Site #31787) Rochester New York 14642 —
Chapel Hill CRS (Site #3201) Chapel Hill North Carolina 27599-7215 —
Cincinnati Clinical Research Site (Site #2401) Cincinnati Ohio 45267-0405 —
Case Clinical Research Site (Site #2501) Cleveland Ohio 44106 —
Ohio State University CRS (Site #2301) Columbus Ohio 43210-1282 —
Penn Therapeutics CRS (Site #6201) Philadelphia Pennsylvania 19104 —
University of Pittsburgh CRS (Site #1001) Pittsburgh Pennsylvania 15213 —
Vanderbilt Therapeutics (VT) CRS (Site #3652) Nashville Tennessee 37204 —
Houston Advancing Research Team CRS (Site #31473) Houston Texas 77030 —
University of Washington Positive Research CRS (Site #1401) Seattle Washington 98104 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07881809, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 19, 2026 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07881809 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →